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首页> 外文期刊>Regulatory Mechanisms in Biosystems >Synthetic positive controls for ELISA test kits for detection of IgA and IgM antibodies to Chlamydia trachomatis
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Synthetic positive controls for ELISA test kits for detection of IgA and IgM antibodies to Chlamydia trachomatis

机译:用于沙眼衣原体IgA和IgM抗体检测的ELISA测试试剂盒的合成阳性对照

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摘要

The enzyme-linked immunosorbent assay (ELISA) is the most informative and versatile method of serological diagnostics. The possibility of detecting by ELISA specific antibodies of different classes allow to differentiate primary infectious process and its remission, exacerbation and chronic disease (holding of differential diagnosis). This approach is implemented in the methodology for evaluation of patients for presence of humoral immune response against the causative agent of urogenital chlamydiosis. As with other infections immediately after Chlamydia trachomatis infection the specific IgM antibodies are formed, and subsequently basic projective antibodies of IgG class are synthesized. However, at exacerbation of chronic urogenital chlamydiosis specific IgA antibodies can be synthesized. That is why comprehensive evaluation of patients for presence of humoral immune response to Ch. trachomatis involves plasma testing of specific antibodies of all three classes. The?essential problem in the production of ELISA diagnostic kits is obtaining of positive control. The classic version of positive control is human blood plasma containing specific antibodies. But specific IgM- and IgA-positive sera are deficit raw materials. This fact can significantly limit the production of diagnostic kits, especially in case of large-scale manufacture. We have suggested methodological approach to use of synthetic positive controls in indirect ELISA kits based on conjugate of normal human IgM (IgA) and monoclonal antibodies against major outer membrane protein of Ch. trachomatis. It was found that it’s possible to realize such task by means of NHS ester-maleimide-mediated conjugation (by sulfosuccinimidyl-4-(N-maleimidomethyl)cyclohexane-1-carboxylate) and reductive amination-mediated conjugation (by sodium periodate). It was found that synthetic positive controls obtained by different methods are characterized by higher titer compared to IgM- and IgA-positive high-titer serum. However, positive control obtained by NHS ester-mediated maleimide conjugation has the best titration profile characteristics, at the release time and after one-week storage at37 °C.
机译:酶联免疫吸附测定(ELISA)是最有用,最通用的血清学诊断方法。通过ELISA检测不同类别的特异性抗体的可能性允许区分原发性感染过程及其缓解,恶化和慢性疾病(进行鉴别诊断)。该方法在评估患者针对泌尿生殖道衣原体病病原体的体液免疫反应存在的方法学中得以实施。与沙眼衣原体感染后立即发生的其他感染一样,形成特异性IgM抗体,随后合成IgG类碱性投射抗体。但是,在慢性泌尿生殖系统衣原体病恶化时,可以合成特异性IgA抗体。这就是为什么要全面评估患者对Ch的体液免疫反应的原因。沙眼包括对所有三类特异性抗体的血浆测试。 ELISA诊断试剂盒生产中的基本问题是获得阳性对照。阳性对照的经典版本是包含特定抗体的人血浆。但是特定的IgM和IgA阳性血清是缺乏的原料。这个事实可能会严重限制诊断套件的生产,特别是在大规模生产的情况下。我们建议了基于正常人IgM(IgA)和针对Ch。主要外膜蛋白的单克隆抗体结合物的间接ELISA试剂盒中使用合成阳性对照的方法学方法。沙眼发现可以通过NHS酯-马来酰亚胺介导的偶联(通过磺基琥珀酰亚胺基-4-(N-马来酰亚胺基甲基)环己烷-1-羧酸)和还原性胺化介导的偶联(通过高碘酸钠)来实现这一任务。发现与IgM和IgA阳性高滴度血清相比,通过不同方法获得的合成阳性对照的滴度更高。但是,通过NHS酯介导的马来酰亚胺偶联获得的阳性对照在释放时和在37°C储存一周后具有最佳的滴定曲线特征。

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